• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

色素失禁症的眼部表现。

Ocular manifestations of incontinentia pigmenti.

作者信息

Holmström G, Thorén K

机构信息

Department of Ophthalmology, Academic Hospital, Uppsala, Sweden.

出版信息

Acta Ophthalmol Scand. 2000 Jun;78(3):348-53. doi: 10.1034/j.1600-0420.2000.078003348.x.

DOI:10.1034/j.1600-0420.2000.078003348.x
PMID:10893071
Abstract

PURPOSE

The study aimed to evaluate the ocular manifestations in patients with incontinentia pigmenti (IP).

METHODS

Thirty patients from different parts of Sweden participated. Orthoptic and ocular examinations were performed as well as evaluation of refraction and visual acuity.

RESULTS

Ocular manifestations, probably associated with IP, were found in 77% (23/30) of the patients. Thirteen had serious or vision-threatening eye manifestations in one eye, of whom 7 were totally blind in that eye from retinal detachments. Ten patients had minor retinal and/or corneal changes.

CONCLUSION

Ocular lesions in patients with IP may be serious and lead to blindness because of retinal disease. Ophthalmological follow-up is essential in the neonatal period and such a programme is recommended.

摘要

目的

本研究旨在评估色素失禁症(IP)患者的眼部表现。

方法

来自瑞典不同地区的30名患者参与了研究。进行了斜视及眼科检查,以及屈光和视力评估。

结果

77%(23/30)的患者发现了可能与IP相关的眼部表现。13名患者一只眼睛有严重或威胁视力的眼部表现,其中7名因视网膜脱离导致该眼完全失明。10名患者有轻微的视网膜和/或角膜变化。

结论

IP患者的眼部病变可能很严重,并因视网膜疾病导致失明。新生儿期进行眼科随访至关重要,建议开展此类项目。

相似文献

1
Ocular manifestations of incontinentia pigmenti.色素失禁症的眼部表现。
Acta Ophthalmol Scand. 2000 Jun;78(3):348-53. doi: 10.1034/j.1600-0420.2000.078003348.x.
2
Incontinentia pigmenti-associated ocular anomalies of paediatric incontinentia pigmenti patients in China.中国小儿遗传性交界性大疱性表皮松解症患者的伴发眼异常。
Acta Ophthalmol. 2019 May;97(3):265-272. doi: 10.1111/aos.13781. Epub 2018 Aug 3.
3
Incontinentia pigmenti: a rare cause of retinal vasculitis in children.色素失禁症:儿童视网膜血管炎的罕见病因。
Tunis Med. 2008 Dec;86(12):1079-81.
4
[Laser therapy in ocular involvement after diagnosis of incontinentia pigmenti in a child].[儿童色素失禁症诊断后眼部受累的激光治疗]
Arch Argent Pediatr. 2019 Jun 1;117(3):e252-e256. doi: 10.5546/aap.2019.e252.
5
Early management of sight threatening retinopathy in incontinentia pigmenti.遗传性皮肤病致盲性视网膜病变的早期治疗。
Orphanet J Rare Dis. 2020 Aug 27;15(1):223. doi: 10.1186/s13023-020-01509-2.
6
Ophthalmological findings in series of incontinentia pigmenti patients from Serbia.塞尔维亚色素失禁症患者系列的眼科检查结果
Srp Arh Celok Lek. 2010 Mar-Apr;138(3-4):150-3. doi: 10.2298/sarh1004150m.
7
Fluorescein angiographic findings in a male infant with incontinentia pigmenti.一名患有色素失禁症男婴的荧光素血管造影检查结果
J AAPOS. 2007 Oct;11(5):511-2. doi: 10.1016/j.jaapos.2007.03.006. Epub 2007 May 10.
8
Extended Follow-up of Treated and Untreated Retinopathy in Incontinentia Pigmenti: Analysis of Peripheral Vascular Changes and Incidence of Retinal Detachment.未经治疗和治疗后的色素失禁症性视网膜病变的长期随访:外周血管变化分析及视网膜脱离的发生率。
JAMA Ophthalmol. 2015 May;133(5):542-8. doi: 10.1001/jamaophthalmol.2015.22.
9
The blinding mechanisms of incontinentia pigmenti.色素失禁症的致盲机制。
Ophthalmic Genet. 1994 Jun;15(2):69-76.
10
The importance of screening for sight-threatening retinopathy in incontinentia pigmenti.色素失禁症中威胁视力的视网膜病变筛查的重要性。
Pediatr Dermatol. 2004 May-Jun;21(3):242-5. doi: 10.1111/j.0736-8046.2004.21311.x.

引用本文的文献

1
Prevalence and clinical characteristics of incontinentia pigmenti: a nationwide population-based study.色素失禁症的患病率及临床特征:一项基于全国人口的研究。
Orphanet J Rare Dis. 2024 Dec 2;19(1):454. doi: 10.1186/s13023-024-03480-8.
2
Ophthalmologic Presentations of Incontinentia Pigmenti.色素失禁症的眼科表现
J Vitreoretin Dis. 2024 Jan 28;8(2):186-191. doi: 10.1177/24741264241227680. eCollection 2024 Mar-Apr.
3
Familial Exudative Vitreoretinopathy Initially Diagnosed as Incontinentia Pigmenti in an Asymptomatic Teenager: A Case Report.
一名无症状青少年最初被诊断为色素失禁症,后确诊为家族性渗出性玻璃体视网膜病变:病例报告
Case Rep Ophthalmol. 2023 Nov 24;14(1):640-646. doi: 10.1159/000533632. eCollection 2023 Jan-Dec.
4
Extraretinal Fibrovascular Proliferation in a Neonate Possibly Associated with an Gene Variant.新生儿视网膜外纤维血管增生可能与一种基因变异有关。
Turk J Ophthalmol. 2023 Dec 21;53(6):386-389. doi: 10.4274/tjo.galenos.2023.72609. Epub 2023 Nov 27.
5
Retinal Manifestations of Incontinentia Pigmenti: A Case Series of 14 Patients Highlighting the Importance of Intravenous Fluorescein Angiography and the Benefits of Early Laser Photocoagulation.色素失禁症的视网膜表现:14例病例系列,强调静脉荧光素血管造影的重要性及早期激光光凝治疗的益处
J Vitreoretin Dis. 2020 Nov 3;5(1):60-65. doi: 10.1177/2474126420962645. eCollection 2021 Jan-Feb.
6
The Prevalence of Retinal Disease and Associated CNS Disease in Young Patients with Incontinentia Pigmenti.患有色素失禁症的年轻患者的视网膜疾病和相关 CNS 疾病的患病率。
Ophthalmol Retina. 2022 Dec;6(12):1113-1121. doi: 10.1016/j.oret.2022.05.032. Epub 2022 Jun 9.
7
Retinal Neovascularization in Two Patients with Incontinentia Pigmenti.两名色素失禁症患者的视网膜新生血管形成
Clin Cosmet Investig Dermatol. 2022 Apr 29;15:803-808. doi: 10.2147/CCID.S363179. eCollection 2022.
8
Case Report: A Case of Cotton-Wool Spots After Intravitreal Injection of Conbercept in an Infant With Incontinentia Pigmenti.病例报告:1例患有色素失禁症的婴儿玻璃体内注射康柏西普后出现棉絮斑的病例
Front Med (Lausanne). 2021 Dec 21;8:761398. doi: 10.3389/fmed.2021.761398. eCollection 2021.
9
Cluster Analysis of Early Postnatal Biochemical Markers May Predict Development of Retinopathy of Prematurity.早产儿视网膜病变发生的早期生化标志物的聚类分析。
Transl Vis Sci Technol. 2020 Dec 8;9(13):14. doi: 10.1167/tvst.9.13.14. eCollection 2020 Dec.
10
Systemic and ocular manifestations of a patient with mosaic ARID1A-associated Coffin-Siris syndrome and review of select mosaic conditions with ophthalmic manifestations.患者患有 ARID1A 相关的 Coffin-Siris 综合征的系统性和眼部表现,以及具有眼部表现的精选嵌合体疾病的综述。
Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):644-655. doi: 10.1002/ajmg.c.31839. Epub 2020 Sep 5.